Abstract
The synthesis of a series of dinuclear gold hydroxide complexes has been achieved. These complexes of type [{Au(IPr)}2(mu-OH)]X (X =BF4, NTf2, OTf, FABA, SbF6; IPr =2,6-bis(disopropylphenyl)imidazol-2-ylidene; NTf2= bis(trifluoromethanesulfonyl)imidate; OTf = trifluoromethanesulfonate; FABA = tetrakis(pentafluorophenyl)borate) are easily formed in the presence of water and prove highly efficient in the catalytic hydration of nitrites. Their facile formation in aqueous media suggests they are of relevance in gold-catalyzed reactions involving water. Additionally, a series of [Au-(IPr)(NCR)][BR4] (R = alkyl, aryl) ficient in the catalytic hydration of nitrites. Their facile formation in aqueous media suggests they are of relevance in gold-catalyzed reactions involving water. Additionally, a series of [Au-(IPr)(NCR)][BR4] (R= alkyl, aryl) complexes was synthesized as they possibly occur as intermediates in the catalytic reaction mechanism. H-1 and C-13 NMR data as well as key bond lengths obtained by X-ray diffraction studies are compared and reveal an interesting structure activity relationship. The collected data indicate a negligible effect of the nature of the nitrite on the reactivity of [Au(L)(NCR)][X] complexes in catalysis.